What you receive
Rare Disease Report
Using A.I. Algorithms and genomic data, our reports aim to help provide diagnoses for rare diseases and reduce waiting times previously needed for filtering and prioritizing variants.
Learn if your personal genetic variants might influence how your body processes over 120 medications. Build a personalized Treatment plan with the most complete Pharmacogenomic Report on the market.
Why do us support Dazzle4Rare?
One analysis, Unique result
How our Tests will help you find long-term answers
We have created specific reports for several rare diseases and are ready to broaden our researchEpilepsy
It is believed that 30% of the epilepsies have a genetic factor. Genes are hugely complex though. We each have up to 2 million “steps” in our DNA ladders, each of which are different in every one of our 20-25,000 genes. The Stripe2Be test simplifies your genetic complexities. Your individual reports can lead to a much quicker diagnosis of a genetic epilepsy.
We have created specific reports for several rare diseases and are ready to broaden our researchMental health conditions
Lots of mental health conditions can be formed of several separate (but overlapping) health issues, with the causes being a mix of genetics, lifestyle, experiences, and more. Your genetic variations can’t be used to diagnose you with psychiatric illnesses but they can help to improve your understanding of contributing factors. This is why at stripes2be we combine your genetic data with your medical health records to identify correlations with any symptoms.
We have created specific reports for several rare diseases and are ready to broaden our researchNeurodegenerative conditions
There’s a huge interest in how genetics influence neurodegenerative diseases such as Alzheimer’s, Parkinson’s, Spinal Muscular Atrophy (SMA), and Amyotrophic Lateral Sclerosis (ALS). Using your genetic data, we can help identify if genetic markers can reliably identify risk of developing these diseases.
We have created specific reports for several rare diseases and are ready to broaden our researchDoctors and Associations
We strictly follow the American College of Medical Genetics (ACMG) guidelines for the development of new reports. The ACMG is the only professionally-recognized international interdisciplinary professional organization of its kind and where organizations must adhere to extremely high standards for membership.
Who we are
Why the name "Stripe2be”?
If you look closely at our DNA, there are unique links, or “stripes” linking up our helices. These remind us of zebras - which have no colours but like us, have unique Stripes. Our individual Stripes are what make us unique. Being aware of our own individual Stripes can help enable us to optimise our levels of health and wellbeing.
What we do for you
We continue to support you
Your journey doesn’t end with your test results. Your reports carry a huge amount of data all about you, which can be a bit overwhelming. This is why we supply genetic counseling to help you accurately interpret your data and modify your lifestyle (should you need to).
We also have a large global network of accredited rare disease associations and advocacy groups with whom you can connect. This can be great if you want to find other people who might have gone/be going through something similar to you.
What are the stripe2be experience and mission?
In our labs we have analyzed the DNA of more than 90,000 people from around the world to help them better their lives.
Our purpose is to better the lives of millions through the democratisation of genetic data. Through this we help individuals like you find out crucial information about their own DNA to better their own health and we then help organizations develop more precise, effective treatments for people too.